Biomacromolecules · 2012 · 34 citations · 39 references
Natural SciencesBiochemistryPharmacokineticsPolymer ChemistryPolymer EngineeringPolymer MaterialsPolymer FunctionalizationPolymer StructurePolymer SynthesisPolymerization ChemistryPolymerization ProcessesProtein ChemistryAtom Transfer Radical PolymerizationPeptide ConjugatesPharmacokinetic EnhancementPolymer ConjugatesPolymer InitiatorsPolymeric Conjugates
Novel pentafluorophenyl (PFP)-ester-functionalized phosphorylcholine (PC) polymers of different architectures were prepared and conjugated to lysozyme as a model protein. Linear and two-arm poly(2-methacryloyloxyethyl phosphorylcholine) (polyMPC) structures containing PFP functionality at the chain-end were prepared by atom transfer radical polymerization (ATRP) from novel initiators. Additional conjugates were prepared from phosphorylcholine-substituted cyclooctene (PC-COE) polymers containing PFP-ester bearing comonomers. The polymer-protein conjugates were characterized by HPLC, FPLC, and DLS and were seen to retain most (~80% or greater) of their native enzymatic activity. Pharmacokinetic profiles of the polymer-protein conjugates were studied in mice and found to increase the circulation half-life compared with lysozyme alone.
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